Incidence and clinical feature of Myasthenia gravis: A five-year data analysis in Ulaanbaatar, Mongolia

Q4 Neuroscience
Oyunaa Chimedregzen, S. Jambal, M. Rentsenbat, B. Dagvajantsan
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Abstract

Myasthenia gravis (MG) is a rare neuromuscular disorder. Till now, there are no studies on the prevalence and incidence of MG in Mongolia. The current study aimed to elucidate the incidence of MG in Ulaanbaatar, the age of onset, and the gender distribution of Mongolian patients with MG. We conducted a cross-sectional, hospital-based study involving MG patients (n=48) all around Ulaanbaatar from 1 January 2015 to 1 January 2020. The clinical diagnosis was assessed with the Myasthenia Gravis Foundation of America (MGFA) classification system. The disease severity was evaluated by using Osserman’s classification. The diagnosis was confirmed with serological and electrophysiological tests. Statistical analysis was performed using SPSS software. A total of 30 patients with MG were registered for the last five years in Ulaanbaatar. The average annual incidence of MG in Ulaanbaatar was 0.65 per 100,000 populations (95%CI 0.26-1.34), 0.60 in males (95%CI 0.25-1.28), and 0.69 in females (95%CI 0.33-1.46). The cumulative incidence in the study period was 3.2 per 100,000 populations. The ratio of males to females was 1:1,3. The median age for onset of MG was 33 years (ranging from 27 to 46 years); 43.3% of patients had ocular and 56.7% generalized symptoms at the disease onset. Only 23.3% of patients remained with purely ocular symptoms (Osserman I stage). The average incidence of MG between 2015 and 2020 was 6,5 per 1.000.000 population, and the annual incidence was relatively stable. Although ocular and generalized symptoms were observed each in about half of the cases, only one-fourth remained with pure ocular signs at the end of the review period.
重症肌无力的发病率和临床特征:蒙古乌兰巴托5年数据分析
重症肌无力是一种罕见的神经肌肉疾病。到目前为止,蒙古还没有关于MG患病率和发病率的研究。本研究旨在阐明蒙古MG患者在乌兰巴托的发病率、发病年龄和性别分布。我们在2015年1月1日至2020年1月1日期间对乌兰巴托各地的MG患者(n=48)进行了一项基于医院的横断面研究。临床诊断采用美国重症肌无力基金会(MGFA)分类系统。采用Osserman分级法评价疾病严重程度。血清学和电生理检查证实了诊断。采用SPSS软件进行统计分析。乌兰巴托在过去五年中总共登记了30名MG患者。乌兰巴托的MG年平均发病率为每10万人0.65例(95%CI 0.26-1.34),男性0.60例(95%CI 0.25-1.28),女性0.69例(95%CI 0.33-1.46)。研究期间的累计发病率为每10万人3.2例。男女比例为1:1,3。MG发病的中位年龄为33岁(范围从27岁到46岁);43.3%的患者发病时有眼部症状,56.7%有全身性症状。只有23.3%的患者仍然有纯粹的眼部症状(Osserman I期)。2015 - 2020年MG的平均发病率为6.5 / 100万人,年发病率相对稳定。虽然在大约一半的病例中分别观察到眼部和全身症状,但在回顾期结束时,只有四分之一的病例仍有纯粹的眼部症状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neuroscience Research Notes
Neuroscience Research Notes Neuroscience-Neurology
CiteScore
1.00
自引率
0.00%
发文量
21
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